Canonical Allele Identifier: CA1108867651
Gene: XRCC2 HGNC NCBI

Linked Data

dbSNP Id: rs2098040895
gnomAD v3: 7-152675993-C-G
gnomAD v4: 7-152675993-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152675993C>G , CM000669.2:g.152675993C>G GRCh38
NC_000007.13:g.152373078C>G , CM000669.1:g.152373078C>G GRCh37
NC_000007.12:g.152004011C>G NCBI36
NG_027988.1:g.5173G>C
NG_027988.2:g.5173G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.-48+48G>C ENSP00000513758.1:n.-48+48G>C
ENST00000698507.1:n.107+48G>C
ENST00000359321.2:c.39+48G>C MANE Select ENSP00000352271.1:n.39+48G>C
ENST00000359321.1:c.39+48G>C ENSP00000352271.1:n.39+48G>C
NM_005431.1:c.39+48G>C NP_005422.1:n.39+48G>C
NM_005431.2:c.39+48G>C MANE Select NP_005422.1:n.39+48G>C
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